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A leading company is seeking a Clinical Research Associate II/Senior CRA to support biotech clinical trials. This role offers strong progression opportunities, working on complex studies primarily in oncology and respiratory areas. The ideal candidate will have a Bachelor’s degree and 2-3 years of monitoring experience, ensuring compliance and fostering relationships with study sites.
This range is provided by i-Pharm Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
110,000.00 / yr - $125,000.00 / yr
Clinical Research Associate II / Senior CRA
Location : US
Are you an experienced CRA ready to take the next step in your career — are you ready to contribute to ground-breaking research positively impacting patient care?
Join a collaborative team as a Clinical Research Associate II or Senior CRA, supporting a portfolio of biotech clinical trials. This role involves working on complex studies, primarily in oncology, respiratory, and related therapeutic areas, alongside leading investigators and sponsor representatives.
This is a growing team AND a growing company and so offers strong progression opportunities. This includes tailored and development programmes in place to support growth from CRA to CPM or COM.
CRA II
CRA III
Senior CRA
Must have 2–3 years of on-site monitoring experience at a reputable CRO to join a high-impact team working exclusively with a dedicated sponsor in various therapeutic areas.
Key Responsibilities
Lead Site Visits : Take charge of site qualification, initiation, routine monitoring, and close-out visits for exciting biotech clinical trials.
Ensure Compliance : Be the guardian of ICH-GCP guidelines, regulatory requirements, and study protocols, ensuring everything stays on track throughout the study lifecycle.
Build Relationships : Foster strong connections with study sites, ensuring top-notch data integrity and patient safety every step of the way.
Solve Problems : Take initiative in resolving data queries and actively contribute to clinical study documentation and reports.
Support Key Activities : Play a vital role in feasibility assessments, site activation, and driving patient recruitment efforts to keep studies progressing smoothly.
About You
Why Apply?
Looking for a role where your experience is valued, and your career can thrive? Let’s connect.
Apply now or reach out directly to learn more.
Seniority level
Seniority level
Not Applicable
Employment type
Employment type
Full-time
Job function
Job function
Research and Science
Research Services and Operations Consulting
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Inferred from the description for this job
401(k)
Vision insurance
Medical insurance
Pension plan
Tuition assistance
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